Comparing two pain relief methods after cesarean section
Comparison of Modified Perichondral Approach Thoracoabdominal Nerve Block and Transversus Abdominal Plane Block in Analgesia Management Following Caesarean Section Surgery
NA · Bursa City Hospital · NCT06185725
This study is testing two different pain relief methods after cesarean section surgery to see which one helps women feel better with less need for opioids.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | Female |
| Sponsor | Bursa City Hospital (other gov) |
| Locations | 1 site (Bursa) |
| Trial ID | NCT06185725 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of two analgesic techniques, the Modified Perichondral Approach Thoracoabdominal Nerve Block and the Transversus Abdominal Plane Block, for managing postoperative pain following cesarean section surgery. Cesarean sections are common surgical procedures, and many women experience moderate to severe pain afterward, which can hinder recovery and affect maternal bonding. By evaluating these two methods, the study seeks to determine which provides better pain relief and reduces the need for opioids. The study will include women undergoing elective cesarean sections who meet specific health criteria.
Who should consider this trial
Good fit: Ideal candidates for this study are women classified as ASA II who are undergoing elective cesarean sections at or beyond 37 weeks of gestation.
Not a fit: Patients with bleeding disorders, those on anticoagulant therapy, or individuals with allergies to local anesthetics or opioids may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for women after cesarean sections, enhancing recovery and maternal well-being.
How similar studies have performed: Previous studies have shown success with regional analgesia techniques like TAP blocks in reducing postoperative pain, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * American Society of Anesthesiologists (ASA) classification II * Elective cesarean section, and gestational age above 37 weeks will be included Exclusion Criteria: * Bleeding diathesis * Anticoagulant treatment * Local anesthetics and opioid allergy * Infection at the site of block * Patients who do not accept the procedure
Where this trial is running
Bursa
- T.C. Sağlık Bakanlığı Bursa Şehir Hastanesi — Bursa, Turkey (RECRUITING)
Study contacts
- Study coordinator: Mursel Ekinci
- Email: drmurselekinci@gmail.com
- Phone: +905067137596
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Cesarean Section, Cesarean Section Pain, Postoperative Analgesia, Transversus Abdominal Plane Block, Modified Perichondral Approach Thoracoabdominal Nerve Block